Novartis

Content Marketing Manager

• Develop and maintain global labelling strategies and core labelling documents for assigned products (e.g. CDS, USPI, EU SmPC/PIL).
• Lead and facilitate cross-functional discussions to support alignment on labelling content and strategy.
• Present labelling proposals and updates to governance bodies and project teams.
• Identify emerging labelling considerations and contribute to planning, risk assessment, and mitigation strategies.
• Analyse competitor labelling, regulatory guidance, and scientific data to inform content development.
• Support and contribute to responses to Health Authority queries and interactions, including preparation of supporting documentation.
• Collaborate with global and regional partners to ensure consistency and alignment across markets.
• Mentor colleagues and contribute to audit readiness, inspections, and continuous improvement initiatives.

Global Labelling Associate Director, Content – Oncology

• Develop and maintain global labelling strategies and core labelling documents for assigned products
• Lead and facilitate cross-functional discussions to support alignment on labelling content and strategy
• Present labelling proposals and updates to governance bodies and project teams
• Identify emerging labelling considerations and contribute to planning, risk assessment, and mitigation strategies
• Collaborate with global and regional partners to ensure consistency and alignment across markets
• Mentor colleagues and contribute to audit readiness, inspections, and continuous improvement initiatives

Global Labelling Associate Director, Content – Established Products

• Act as labelling lead for assigned products, developing and maintaining global core labelling documents and major market labels (e.g. CDS, USPI, EU SmPC/PIL)
• Organise and facilitate cross-functional labelling discussions (e.g. ELTF meetings) to support alignment on content
• Collaborate with Global Labelling colleagues and cross-functional teams to ensure consistent, compliant, and competitive labelling content
• Conduct research across competitor labels, regulatory guidance, and clinical data to inform labelling updates
• Prepare documentation to support labelling changes and contribute to responses to Health Authority queries
• Support timely implementation of labelling updates across countries, ensuring alignment with global standards
• Maintain high-quality documentation, including version control, references, and rationale for changes
• Support audit and inspection readiness, mentoring colleagues where appropriate, and contributing to continuous improvement initiatives

Global Labelling Manager, Content – Neuroscience

QA Engineer

• Responsible for QA release activities in context of raw material and consumables release.
• Handling of quality relevant events (DEV, OOx, complaints, etc.).
• Support monitoring, tracking and evaluation of the material release setup, contribute to the IIA KPI and RCI processes.
• Lead and support DEV, OOx and complaint investigations and promote quality relevant topics and projects in scope.
• Ensure timely and compliant release of raw material & consumables.
• Drive consistent and efficient operation of the quality operations function in the area of responsibility.
• Seek opportunities for productivity improvements, and coordinate their implementation.

QA Operations Expert

Attorney

• Provide strategic intellectual property guidance to research and development teams, protecting inventions and reducing third‑party risk
• Build and steer patent portfolios aligned to scientific strategy, product milestones, and long‑term value
• Draft, file, prosecute, and maintain patent applications across United States and international jurisdictions
• Provide opinions on patentability, validity, and freedom to operate to guide decisions
• Shape publication and disclosure strategies balancing scientific visibility with robust protection and exclusivity options
• Lead due diligence, risk evaluation, and mitigation for collaborations, licensing opportunities, and transactional projects
• Partner with global colleagues and external counsel to deliver quality work on time and budget

Patent Attorney

Research Analyst

• Build strong partnerships with clinical trial sites
• Manage assigned sites across Phase One to Phase Four trials
• Lead site initiation visits and ensure site teams are fully trained
• Conduct remote and on-site monitoring activities
• Evaluate site performance proactively and implement mitigation plans
• Drive early site engagement through feasibility activities
• Maintain complete and accurate study documentation
• Support inspection readiness through audit preparation
• Identify operational improvement opportunities and work with sites

Clinical Research Associate III

Sales

• Handle delivering sales performance and promoting product(s) within oncology, hematology or rare disease portfolio
• Collaborate cross functionally in each geography as ONE team
• Execute call-plan to achieve goals and improve access and sales opportunities
• Use sales data reporting tools to understand trends and customer insights
• Develop and execute account level plans

Oncology Sales Specialist, Malignant Hematology

Operations

• Serve as the strategic operations lead on the Market Access Channel Strategy team
• Design and implement innovative channel operations and market access field engagement models
• Lead the development and implementation of operational models to support CGT and RLT product distribution, dispensing, pricing, contracting, and business-to-business field engagement strategies
• Support the creation of commercial data and field strategies to enable strategic pull through, monitoring, and improvement to channel strategies
• Directly guide implementation of account pricing, channel contracting, leading the negotiation and implementation of channel programs for assigned accounts in collaboration with finance, contracting, and trade operations teams
• Create operational strategy and solutions that meet both external customer and Novartis business needs

Director, Channel Operations Strategy – Advanced Platforms

Data Analyst

• Support DM Leads and Data Quality Teams (DQT) in deriving and articulating both planned and ad-hoc clinical and operational data insights.
• Drive cross-functional collaboration to enhance data strategy, quality, site experience, and patient safety using disease area, protocol, and data standards expertise.
• Partner with Central Monitoring (CM) and Risk-based Quality Management (RbQM) leads to promote risk-based data review approaches.
• Act as a data review solution advisor, translating complex insights into clear, actionable recommendations for stakeholders.
• Contribute to exploratory data quality management plans in collaboration with DQT.
• Enable detection of data discrepancies and anomalies by supporting deployment of user-friendly analytical tools.
• Promote responsible AI adoption, develop proof-of-concepts (PoCs), and support product ionization of approved use cases.
• Identify opportunities to optimize analytics processes and improve solution performance.
• Stay current with emerging technologies, trends, and best practices in data analytics, automation, and AI.
• Develop and maintain technical documentation while fostering a culture of innovation and continuous learning.

Clinical Data Analytics Lead

Director

• Act as the primary interface between business stakeholders, biostatisticians, statistical programmers, and technical teams.
• Lead requirement gathering workshops and translate clinical/statistical needs into structured functional and technical specifications.
• Ensure alignment between Statistical Analysis Plans, reporting outputs (TLFs), and system implementation.
• Drive end-to-end requirement traceability across development, validation, and deployment phases.
• Oversee design and delivery of scalable R-based analytics applications and Shiny dashboards.
• Ensure regulatory compliance, audit readiness, and adherence to documentation and governance standards.
• Provide structured updates on progress, risks, dependencies, and mitigation plans.

Associate Director, Technology – Scientific Computing

Manager

• Own end‑to‑end FinOps operations for Medical Affairs, from request intake through closure
• Ensure accurate and compliant PR, PO, and SOW creation, amendments, and issue resolution
• Oversee invoice processing, service confirmations, GR/IR management, and timely payments
• Manage vendor onboarding, amendments, and lifecycle support in partnership with Procurement and Finance
• Ensure timely and accurate accruals, invoice cut‑offs, and month‑end / quarter‑end close activities
• Act as the primary operational escalation point for Medical Affairs finance‑related issues
• Provide operational support to the wider FinOps team based on business demand and priorities
• Support cross‑TA activities such as backlog management, audits, transitions, and special initiatives
• Partner closely with US BPAs, Medical Affairs stakeholders, Procurement, and Finance teams to ensure seamless execution
• Lead, coach, and develop a team of Medical Affairs & FinOps